Medical Device Recalls
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1 result found
510(K) Number: K130794 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CELLTRACKS ANALYZER II® (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II® is a se... | 2 | 03/13/2014 | Veridex, LLC |
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